Allele Registry

Canonical Allele Identifier: PA915973659

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000007055

RCV000007056

RCV000790785

RCV000807968

ClinVar Variation:

6671

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124454.1:p.Pro823Arg	CA222139 NM_001130982.2:c.2468C>G